M&A in Pharmaceuticals: Deal Boom Due to AI Drug Development https://ymaho.com/m-a-in-pharmaceuticals-deal-boom-due-to-ai-drug-development
Big Pharma spends billions on buying AI startups to shorten the R&D cycle. Learn how AI is changing the M&A market. Detailed analysis.
Marne-Cel FDA approval: gene therapy for LAD-I https://ymaho.com/marne-cel-fda-approval-gene-therapy-for-lad-i
FDA approved Marne-Cel for children with severe LAD-I: 100% survival in trials. Learn how Rocket Pharmaceuticals turned rejections into a breakthrough.
Big Pharma Mergers: $84 Billion in Deals in a Quarter https://ymaho.com/big-pharma-mergers-84-billion-in-deals-in-a-quarter
The $300 Billion Patent Cliff Drove Big Pharma to Spend $84 Billion on Biotech Deals in Q1. Find Out Which Companies Are Buying and Why.
Vepdegestrant: the first breast cancer protein degrader https://ymaho.com/vepdegestrant-the-first-breast-cancer-protein-degrader
FDA approved vepdegestrant — the first PROTAC degrader for breast cancer with ESR1 mutation. Learn how it destroys resistance and what will change in therapy. Details here.
Langlara: FDA approved Chinese insulin biosimilar https://ymaho.com/langlara-fda-approved-chinese-insulin-biosimilar
FDA approved interchangeable biosimilar insulin glargine Langlara from Chinese Sunshine Lake. Learn how this will change the US market and prices for patients. Detailed analysis inside.
FDA approved Langlara as an interchangeable biosimilar of insulin glargine https://ymaho.com/fda-approved-langlara-as-an-interchangeable-biosimilar-of-insulin-glargine
FDA granted Langlara interchangeable biosimilar status to Lantus. Learn how this will change the US insulin market and expand patient access to therapy.
SaRNA vaccine for cats: EMA decision as a breakthrough for medicine https://ymaho.com/sarna-vaccine-for-cats-ema-decision-as-a-breakthrough-for-medicine
EMA has approved the first RNA vaccine for animals. We analyze why this decision opens a new wave in human medicine and changes the market. Get insights.
Biosimilar without Phase 3: FDA and EMA Rewrite the Rules https://ymaho.com/biosimilar-without-phase-3-fda-and-ema-rewrite-the-rules
FDA and EMA approved skipping Phase 3 for Herceptin biosimilar AP063. Learn how this decision will change the biosimilar market and accelerate access to cancer therapy.
FDA will approve subcutaneous Lecanemab in August 2026 https://ymaho.com/fda-will-approve-subcutaneous-lecanemab-in-august-2026
Analysis of the FDA decision postponement for Leqembi IQLIK to August 24: why this is a signal for approval, not a delay. Benefits for Alzheimer's patients and market forecast. Read key takeaways.
FDA may approve ophthalmic bevacizumab Lytenava https://ymaho.com/fda-may-approve-ophthalmic-bevacizumab-lytenava
Analysis of the regulatory paradox: why the FDA rejected it three times, while Europe approved it. Learn how the Lytenava decision will change the $16 billion AMD market.